Canonical Allele Identifier: CA404122809

Gene: ODAD3

Linked Data

• dbSNP Id: rs1289891684
• gnomAD v2: 19-11536981-C-G
• gnomAD v4: 19-11426161-C-G
• MyVariant Identifiers: chr19:g.11536981C>G (hg19) ; chr19:g.11426161C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11426161C>G , CM000681.2:g.11426161C>G	GRCh38
NC_000019.9:g.11536981C>G , CM000681.1:g.11536981C>G	GRCh37
NC_000019.8:g.11397981C>G	NCBI36
NG_041777.1:g.14622G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356392.9:c.946G>C MANE Select	ENSP00000348757.3:p.Glu316Gln
ENST00000356392.8:c.946G>C	ENSP00000348757.3:p.Glu316Gln
ENST00000586836.5:c.373G>C	ENSP00000467429.1:p.Glu125Gln
ENST00000591179.5:c.766G>C	ENSP00000466800.1:p.Glu256Gln
ENST00000591345.5:c.*865G>C	ENSP00000467313.1:n.*865G>C
NM_001302453.1:c.784G>C	NP_001289382.1:p.Glu262Gln
NM_001302454.1:c.766G>C	NP_001289383.1:p.Glu256Gln
NM_145045.4:c.946G>C	NP_659482.3:p.Glu316Gln
XM_017026241.1:c.904+42G>C	XP_016881730.1:n.904+42G>C
NM_145045.5:c.946G>C MANE Select	NP_659482.3:p.Glu316Gln
NM_001302454.2:c.766G>C	NP_001289383.1:p.Glu256Gln